Matt Baker

24.3k citations

83 papers · 5.1k · 1 hit paper · h-index 38

Impact in

Neurology top 0.1%
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research

Papers in

Neurology 50
- Amyotrophic Lateral Sclerosis Research 38
- Parkinson's Disease Mechanisms and Treatments 22
- Neurological diseases and metabolism 19
Physiology 24
- Alzheimer's disease research and treatments 24

Co-authors: Rosa Rademakers (52 shared papers)Manuela Neumann (5 shared papers)Sigrun Roeber (2 shared papers)I. R. A. Mackenzie (3 shared papers)Mike Hutton (14 shared papers)H. A. Kretzschmar (1 shared paper)Dennis W. Dickson (20 shared papers)Ian R. Mackenzie (12 shared papers)
Journals: Neurology (14 papers)Acta Neuropathologica (7 papers)Annals of Neurology (7 papers)European Journal of Neurology (3 papers)Journal of Neuropathology & Experimental Neurology (3 papers)
Partner nations: United States Canada United Kingdom

In The Last Decade

Matt Baker

81 papers receiving 5.1k citations

Matt Baker's Hit Papers

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A new subtype of frontotemporal lobar degeneration with FUS pathology 2009 · 547 citations

Peers

Countries citing papers authored by Matt Baker

Since Specialization

Citations

This map shows the geographic impact of Matt Baker's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Matt Baker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matt Baker more than expected).

Fields of papers citing papers by Matt Baker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matt Baker. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Matt Baker. The network helps show where Matt Baker may publish in the future.

Co-authors

The 25 scholars most cited alongside Matt Baker, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Matt Baker Line = papers co-authored together Matt Baker links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 83 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A new subtype of frontotemporal lobar degeneration with FUS pathology Brain ·Manuela Neumann, Rosa Rademakers, Sigrun Roeber, Matt Baker, H. A. Kretzschmar, I. R. A. Mackenzie Hit paper breakdown →	2009	547
2	TDP‐43 A315T mutation in familial motor neuron disease Annals of Neurology ·Michael A. Gitcho, Robert H. Baloh, Sumi Chakraverty, Kevin H. Mayo, Joanne Norton, Denise Levitch, Kimmo J. Hatanpaa, Charles L. White, Eileen H. Bigio, Richard J. Caselli, Matt Baker, Muhammad Al‐Lozi, John C. Morris, Alan Pestronk, Rosa Rademakers, Alison Goate, Nigel J. Cairns	2008	498
3	A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1 Nature Medicine ·Richard Crook, Auli Verkkoniemi, Jordi Pérez‐Tur, Nitin D. Mehta, Matt Baker, Henry Houlden, Matthew J. Farrer, Mike Hutton, Sarah Lincoln, John Hardy, Katrina Gwinn, Mirja Somer, Anders Paetau, Hannu Kalimo, Raija Ylikoski, Minna Pöyhönen, Steve Kucera, Matti Haltia	1998	266
4	5′ Splice Site Mutations in tau Associated with the Inherited Dementia FTDP-17 Affect a Stem-Loop Structure That Regulates Alternative Splicing of Exon 10 Journal of Biological Chemistry ·Andrew Grover, Henry Houlden, Matt Baker, Jennifer Adamson, Jada Lewis, Guy Prihar, Stuart Pickering‐Brown, Karen Duff, Mike Hutton	1999	240
5	Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72 Acta Neuropathologica ·Melissa E. Murray, Mariely DeJesus‐Hernandez, Nicola J. Rutherford, Matt Baker, Ranjan Duara, Neill R. Graff‐Radford, Zbigniew K. Wszołek, Tanis J. Ferman, Keith A. Josephs, Khrista Boylan, Rosa Rademakers, Dennis W. Dickson	2011	227
6	Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype Neurology ·Keith A. Josephs, Jennifer L. Whitwell, David S. Knopman, William T. Hu, David Alexander Stroh, Matt Baker, Rosa Rademakers, Bradley F. Boeve, Joseph E. Parisi, Glenn E. Smith, Robert J. Ivnik, Ronald C. Petersen, Clifford R. Jack, Dennis W. Dickson	2008	207
7	Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease Acta Neuropathologica ·Manuela Neumann, Sigrun Roeber, Hans A. Kretzschmar, Rosa Rademakers, Matt Baker, Ian R. Mackenzie	2009	199
8	Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p Brain ·Ging‐Yuek Robin Hsiung, M. DeJesus-Hernandez, Howard Feldman, Pheth Sengdy, P. Bouchard-Kerr, E. Dwosh, Rachel Butler, Bonnie Leung, A. Fok, Nicola J. Rutherford, Matt Baker, Rosa Rademakers, I. R. A. Mackenzie	2012	162
9	Frontotemporal dementia due toC9ORF72mutations Neurology ·Sharon J. Sha, Leonel Tadao Takada, Katherine P. Rankin, Jennifer S. Yokoyama, Nicola J. Rutherford, Jamie Fong, Baber K. Khan, Anna Karydas, Matt Baker, Mariely DeJesus‐Hernandez, Mochtar Pribadi, Giovanni Coppola, Daniel H. Geschwind, Rosa Rademakers, Suzee E. Lee, William W. Seeley, Bruce L. Miller, Adam L. Boxer	2012	148
10	Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation Acta Neuropathologica ·Ian R. Mackenzie, Olaf Ansorge, Michael J. Strong, Juan M. Bilbao, Lorne Zinman, Lee‐Cyn Ang, Matt Baker, Heather Stewart, Andrew Eisen, Rosa Rademakers, Manuela Neumann	2011	141
11	De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis Human Mutation ·Mariely DeJesus‐Hernandez, Jannet Kocerha, NiCole A. Finch, Richard Crook, Matt Baker, Pamela Desaro, Amelia Johnston, Nicola J. Rutherford, Aleksandra Wojtas, Kathleen D. Kennelly, Zbigniew K. Wszołek, Neill R. Graff‐Radford, Khrista Boylan, Rosa Rademakers	2010	128
12	Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p Acta Neuropathologica ·Heather Stewart, Nicola J. Rutherford, Hannah Briemberg, Charles Krieger, Neil R. Cashman, Marife Fabros, Matt Baker, Alice Fok, Mariely DeJesus‐Hernandez, Andrew Eisen, Rosa Rademakers, Ian R. Mackenzie	2012	126
13	CSF1R mutations link POLD and HDLS as a single disease entity Neurology ·Alexandra M. Nicholson, Matt Baker, NiCole A. Finch, Nicola J. Rutherford, Christian Wider, Neill R. Graff‐Radford, Peter T. Nelson, H. Brent Clark, Zbigniew K. Wszołek, Dennis W. Dickson, David S. Knopman, Rosa Rademakers	2013	121
14	Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma The American Journal of Human Genetics ·Minerva M. Carrasquillo, Alexandra M. Nicholson, NiCole A. Finch, J. Raphael Gibbs, Matt Baker, Nicola J. Rutherford, Talisha A. Hunter, Mariely DeJesus‐Hernandez, Gina Bisceglio, Ian R. Mackenzie, Andrew Singleton, Mark Cookson, Julia E. Crook, Allissa Dillman, Dena G. Hernandez, Ronald C. Petersen, Neill R. Graff‐Radford, Steven G. Younkin, Rosa Rademakers	2010	112
15	Altered functional connectivity in asymptomatic MAPT subjects Neurology ·Jennifer L. Whitwell, Keith A. Josephs, Ramesh Avula, Nirubol Tosakulwong, Stephen D. Weigand, Matthew L. Senjem, Prashanthi Vemuri, David T. Jones, Jeffrey L. Gunter, Matt Baker, Zbigniew K. Wszołek, David S. Knopman, Rosa Rademakers, R. C. Petersen, B. F. Boeve, Clifford R. Jack	2011	101
16	Frequency oftau mutations in three series of non-Alzheimer's degenerative dementia Annals of Neurology ·Henry Houlden, Matt Baker, Joy Adamson, Andrew Grover, Stephen C. Waring, Dennis W. Dickson, Timothy Lynch, Bradley F. Boeve, R. C. Petersen, Stuart Pickering‐Brown, F. Owen, David Neary, David Craufurd, Julie S. Snowden, D.M.A. Mann, M. Hutton	1999	100
17	Pick's disease is associated with mutations in thetau gene Annals of Neurology ·Stuart Pickering‐Brown, Matt Baker, Shu‐Hui Yen, Wan-Kyng Liu, Masato Hasegawa, Nigel J. Cairns, P. L. Lantos, Martin N. Rossor, Takeshi Iwatsubo, Yvonne Davies, David Allsop, Rob Furlong, F. Owen, John Hardy, David Mann, Mike Hutton	2000	99
18	Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease Neuroreport ·Sarah Lincoln, Jenny Vaughan, (unknown), Matt Baker, Jennifer Adamson, Katrina Gwinn, Timothy Lynch, John Hardy, Matthew J. Farrer	1999	90
19	Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images European Journal of Neurology ·Jennifer L. Whitwell, Bradley F. Boeve, Stephen D. Weigand, Matthew L. Senjem, Jeffrey L. Gunter, Matt Baker, Mariely DeJesus‐Hernandez, D. S. Knopman, Z. Wszolek, R. C. Petersen, R. Rademakers, Clifford R. Jack, Keith A. Josephs	2015	75
20	A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch Neurobiology of Disease ·Zareen Amtul, Patrick A. Lewis, Siân C. Piper, Richard Crook, Matt Baker, Kirk A. Findlay, Andrew Singleton, Marion C. Hogg, Linda H. Younkin, Steven G. Younkin, John Hardy, Michael Hutton, Bradley F. Boeve, David F. Tang‐Wai, Todd E. Golde	2002	75

About Matt Baker

Matt Baker is a scholar working on Neurology, Physiology, Neurology, Molecular Biology and Genetics, having authored 83 papers that have together received 5.1k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (38 papers), Alzheimer's disease research and treatments (24 papers), Parkinson's Disease Mechanisms and Treatments (22 papers), Neurological diseases and metabolism (19 papers), Neurogenetic and Muscular Disorders Research (9 papers), Prion Diseases and Protein Misfolding (8 papers), RNA Research and Splicing (4 papers) and Genetic Neurodegenerative Diseases (4 papers). The work is most often cited by research in Neurology (3.2k citations), Neurology (1.1k citations), Genetics (990 citations), Physiology (1.9k citations) and Cellular and Molecular Neuroscience (628 citations). Matt Baker has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Rosa Rademakers, Manuela Neumann, Sigrun Roeber, I. R. A. Mackenzie, Mike Hutton, H. A. Kretzschmar, Dennis W. Dickson, Ian R. Mackenzie, Nicola J. Rutherford and Neill R. Graff‐Radford. Their work appears in journals such as Neurology, Acta Neuropathologica, Annals of Neurology, European Journal of Neurology and Journal of Neuropathology & Experimental Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Matt Baker

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Matt Baker

Matt Baker's Hit Papers

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About Matt Baker

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